Protocol for a process evaluation of SCALA study:Intervention targeting scaling up of primary health care-based prevention and management of heavy drinking and comorbid depression in Latin America

Autor: Daša Kokole, Eva Jané-Llopis, Liesbeth Mercken, Guillermina Natera Rey, Miriam Arroyo, Augusto Pérez Gómez, Juliana Mejía-Trujillo, Marina Piazza, Ines Bustamante, Amy O’Donnell, Eileen Kaner, Bernd Schulte, Hein de Vries, Peter Anderson
Přispěvatelé: Department of Health Psychology, RS-Research Line Health psychology (part of UHC program), RS: CAPHRI - R6 - Promoting Health & Personalised Care, Health promotion
Jazyk: angličtina
Rok vydání: 2023
Předmět:
Zdroj: Kokole, D, Jané-Llopis, E, Mercken, L, Natera Rey, G, Arroyo, M, Pérez Gómez, A, Mejía-Trujillo, J, Piazza, M, Bustamante, I, O'Donnell, A, Kaner, E, Schulte, B, de Vries, H & Anderson, P 2023, ' Protocol for a process evaluation of SCALA study : Intervention targeting scaling up of primary health care-based prevention and management of heavy drinking and comorbid depression in Latin America ', Evaluation and Program Planning, vol. 97, 102217 . https://doi.org/10.1016/j.evalprogplan.2022.102217
Evaluation and Program Planning, 97:102217. Elsevier Ltd
Evaluation and Program Planning, 97:102217. Elsevier Science
ISSN: 0149-7189
DOI: 10.1016/j.evalprogplan.2022.102217
Popis: This paper describes the plan for a process evaluation of a quasi-experimental study testing the municipal level scale-up of primary health care-based measurement and brief advice programmes to reduce heavy drinking and comorbid depression in Colombia, Mexico, and Peru. The main aims of the evaluation are to assess the implementation of intervention components; mechanisms of impact that influenced the outcomes; and characteristics of the context that influenced implementation and outcomes. Based on this information, common drivers of successful outcomes will be identified. A range of data collection methods will be used: questionnaires; interviews; observations; logbooks; and document analysis. All participating providers will complete a pen-and-paper questionnaire at recruitment and two time points during the implementation period. Providers attending training will complete post-training questionnaires. Additionally, 1080 patients will be invited to self-complete a patient questionnaire. One-in-ten participating providers and fifteen other key stakeholders will participate in semi-structured interviews. Training sessions and community advisory board meetings will be observed by a neutral observer. Logbooks will be kept by local research teams to document events affecting the implementation. Project related documentation and other relevant reports describing the context will be examined.
Databáze: OpenAIRE